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HOME > Urogenit Tract Infect > Volume 18(3); 2023 > Article
Case Report Case of Life-Threatening Pneumonia during the Treatment of a Patient with Acute Bacterial Prostatitis
Kyung Kgi Parkorcid, Sung Dae Kimorcid, Young-Joo Kimorcid, Jung-Sik Huhorcid
Urogenital Tract Infection 2023;18(3):114-118.
DOI: https://doi.org/10.14777/uti.2023.18.3.114
Published online: December 31, 2023

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Correspondence to: Jung-Sik Huh, https://orcid.org/0000-0003-2767-4390' target='_blank'>orcid , Department of Urology, Jeju National University Hospital, School of Medicine, Jeju National University, 15 Aran 13-gil, Jeju 63241, Korea, Tel: +82-64-717-1760, Fax: +82-64-717-1131, E-mail: urohjs@jejunu.ac.kr">urohjs@jejunu.ac.kr
• Received: October 25, 2023   • Revised: November 26, 2023   • Accepted: December 3, 2023

Copyright © 2023, Korean Association of Urogenital Tract Infection and Inflammation. All rights reserved.

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This article has been corrected. See "Correction: Addendum of Informed Consent Statements" in Volume 19 on page 109.
  • Acute bacterial prostatitis is an acute urinary tract infection associated with a bladder outlet obstruction or an immunosuppressed state. A 51-year-old man patient visited the hospital with fever, chills, and acute urinary retention that started the day before his visit after consuming a significant amount of alcohol. Conservative treatments, including catheterization for urinary drainage and antibiotics, were performed. On the third day of treatment for acute prostatitis, he complained of dyspnea. The level of oxygen differentiation was reduced significantly, and the tracheal insertion and ventilator were maintained after the radiological examination. The ventilator was discontinued, and the prostate abscess was operated on the eighth day of hospitalization. He was discharged without complications. This paper reports a case of life-threatening pneumonia and a prostate abscess during the treatment of a patient with acute bacterial prostatitis with a review of the relevant literature.
Acute bacterial prostatitis (ABP) is an acute urinary tract infection associated with a bladder outlet obstruction or an immunosuppressed state that can occur in males of any age. The progression of ABP can occur in a variety of ways depending on the patient’s chronic disease and treatment time [1]. A prostate abscess is a rare complication of the treatment for acute prostatitis [2]. The most common strains of this disease are Escherichia coli (E. coli). Klebsiella pneumoniae (K. pneumoniae), and Staphylococcus [3-5]. K. pneumoniae is a member of the Enterobacteriaceae family and is an opportunistic pathogen that causes pneumonia, bacteremia, and urinary tract infections depending on the patient’s health condition [6].
This paper reports a case of life-threatening pneumonia and a prostatic abscess that occurred during the treatment of a patient with ABP caused by K. pneumoniae with a review of the relevant literature.
A 51-year-old man had a prior medical history of cholecystectomy caused by a gallbladder stone without chronic disease, such as diabetes mellitus and hypertension. He presented at the emergency department with fever, dysuria, hesitancy, and acute urinary retention one day ago after consuming a considerable amount of alcohol.
The laboratory data revealed the following serum levels: white blood cells (WBCs) of 13.36×103/μl, 1.40 mg/dl creatinine, 127 mmol/L sodium, C-reactive protein of 30.19 mg/dl, erythrocyte sedimentation rate of 120 mm/hr, and WBC and red blood cells of many/high-pass filter in the urine. The initial chest posteroanterior (PA) revealed no active lung lesion (Fig. 1A). Computed tomography (CT) of the abdomen and pelvis showed no gall bladder and an enlarged prostate (Fig. 2A). He underwent a 16 Fr foley catheter and received sodium replacement and Pipe-racillin/Tazobactam 4.5 g IV tid for three days. On the second day of hospitalization, transrectal ultrasound showed no evidence of a prostate abscess except for an enlarged prostate (Fig. 3). On the third day of hospitalization, the patient complained of dyspnea. His general condition gradually deteriorated, and his blood pressure, heart rate, respiratory rate, and body temperature were 96/47 mmHg, 142/min, 35/min, and 38.6°C, respectively. The chest X-ray (Fig. 1B) showed newly appeared diffuse patchy and nodular opacities throughout both lungs. The common blood counts and arterial blood analysis revealed a platelet count of 16×103 counts/mm3, partial pressure of oxygen level of 59.6 mmHg, partial pressure of carbon dioxide of 30.2 mmHg, and potential hydrogen of 7.43. A CT scan of the chest showed dense consolidation in both lobes (Fig. 4). He was under severe respiratory distress, and his blood pressure decreased. Subsequently, a vasopressor was used to increase his blood pressure. The antibiotic was changed (meropenem 2 g for three days), and a ventilator was inserted in the intensive care unit. The culture of blood and urine yielded K. pneumoniae (Table 1). The patient’s conscious state changed, but there was no significant lesion on the magnetic resonance imaging scan of the brain.
The patient’s blood pressure was maintained, and the vasopressor was gradually decreased. On the sixth day of admission to the intensive care unit, the vasopressor was discontinued. A CT scan of the abdomen and pelvis demonstrated multiple loculated fluid collections and a lobulated lesion in the prostate (Fig. 2B). The prostate abscess was drained by transurethral unroofing of the prostate on the eighth day of admission to the intensive care unit (Fig. 5). The patient’s spontaneous respiration was maintained, and the ventilator was discontinued on the 10th day. The patient was then transferred to the general ward on the 13th day. The pathology result of the prostate was suppurative inflammation. He was discharged with full recovery after 19 days of admission. Four weeks after discharge, transrectal ultrasound revealed a reduced prostate volume (Fig. 6). He did not complain of voiding symptoms, and no complications had occurred nine months after discharge. Authors received informed consent for the use of the patients’ photographs or other information through the publication.
ABP is an acute urinary tract infection that can happen at any age but occurs frequently among patients with immunocompromised status and becomes increasingly common with age [1,7]. ABP has a variety of outcomes depending on the patient’s condition or chronic disease, and a prostate abscess may occur [2,5]. Among various chronic diseases, diabetes mellitus is one of the risk factors for a prostate abscess. Delaying the diagnosis and treatment of prostate abscess increases the mortality rate [2,7].
Symptoms of prostate abscess are voiding symptoms, including dysuria, tenesmus, and urinary retention accompanied by fever or perineal discomfort [8]. In this case, the patient visited the emergency room with fever, dysuria, and acute urinary retention.
The strains causing prostatic abscesses include E. coli, K. pneumoniae, and Staphylococcus [3-5]. A previous study reported E. coli in four cases, K. pneumoniae in three cases, and Staphylococcus aureus in one case [5]. In the present case, K. pneumoniae was identified in the urine and blood culture.
K. pneumoniae is an opportunistic pathogen that causes pneumonia (rare primary pneumonia but nosocomial pneumonia) and hospital-acquired urinary tract infections [7,9]. The occurrence of bacteremia and urinary tract infections depends on the patient’s health condition [6].
One study reported a 60-year-old man with diabetes, previously treated for ABP, who had developed a prostate abscess caused by K. pneumoniae, complicating septic pulmonary emboli and meningitis [7]. Acute respiratory distress syndrome (ARDS) is a life-threatening condition caused by bacteremia or viruses and can result from infectious diseases that have worsened [10].
In the present case, a patient with no diabetes mellitus used the appropriate antibiotics (Piperacillin/Tazobactam) according to the results of a previous study [5]. He also had no respiratory symptoms at the time of hospitalization and no abnormality in the chest PA examination. He was treated immediately on the day the symptoms appeared. On the third day of hospitalization, he deteriorated rapidly and had ARDS. He recovered completely through conservative treatment with vasopressors, ventilators, transfusions, and antibiotic changes.
In conclusion, physicians should consider the treatment of patients with ABP who do not have chronic diseases, such as diabetes mellitus. Despite using the appropriate antibiotics when the symptoms were recognized, K. pneumoniae from acute prostatitis spread to multi-organs, including the lungs and brain. ARDS could not be suppressed, and the symptoms intensified [7]. Therefore, if a patient is experiencing difficulty breathing or other symptoms, physicians should check the lesions rapidly and treat them through chest and abdominal computed tomography, even before the bacteria can be identified.

CONFLICT OF INTEREST

No potential conflict of interest relevant to this article was reported.

FUNDING

No funding to declare.

AUTHOR CONTRIBUTIONS

K.K.P. participated in data collection and wrote the manuscript. S.D.K., Y.J.K. participated in the study design. J.S.H. participated in the study design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.

Fig. 1
(A) On the first day. Chest posteroanterior (PA): no active lung lesion. (B) On the third day. Chest PA: newly appeared diffuse patchy and nodular opacities throughout both lungs.
uti-18-3-114-f1.jpg
Fig. 2
In the contrast-enhanced com-puted tomography scan. (A) The axial view showed prostatic enlargement with heterogeneous enhancement on the admission day. (B) The axial view demonstrated multiple loculated fluid collections and lobulated lesions in the prostate on the seventh day after hospitalization.
uti-18-3-114-f2.jpg
Fig. 3
On the second day, transrectal ultrasound revealed a prostate volume of 152 gm with central gland enlargement and calcifications, and heterogeneous parenchymal echoes were observed in both peripheral zones.
uti-18-3-114-f3.jpg
Fig. 4
Computed tomography scan of the chest showed dense consolidation in both lobes (pneumonia with acute respiratory distress syndrome).
uti-18-3-114-f4.jpg
Fig. 5
On the eighth day of admission to the intensive care unit, transurethral unroofing of the prostate abscess.
uti-18-3-114-f5.jpg
Fig. 6
Transrectal ultrasound showed that the prostate volume decreased to 27.7 gm one month after discharge.
uti-18-3-114-f6.jpg
Table 1
Antibiotic sensitivity of the bacteria identified in the urine and blood cultures
Urine culture Blood culture
Bacteria Klebsiella pneumoniae Klebsiella pneumoniae
Result of sensitivity Ampicillin/Sulbactame≤8/4 (S) ESBL (-)
Amikacin≤16 (S) Ampicillin≥32 (R)
Ampicillin>16 (R) Amoxicillin/Clavulanic acid≤2 (S)
Aztreonam≤4 (S) Piperacillin/Tazobactam≤4 (S)
Ceftazidime≤1 (S) Ceftizoxime≤4 (S)
Cefotaxime≤1 (S) Cefoxitin≤4 (S)
Cefoxitin≤8 (S) Cefotaxime≤1 (S)
Ceftizoxime≤2 (S) Ceftazidime≤1 (S)
Ciprofloxacin≤1 (S) Cefepime≤1 (S)
Cefepime≤2 (S) Aztreonam≤1 (S)
Cefuroxime≤4 (S) Ertapenem≤0.5 (S)
Ertapenem≤0.5 (S) Imipenem≤0.3 (S)
Gentamicin≤4 (S) Amikacin≤2 (S)
Imipenem≤1 (S) Gentamicin≤1 (S)
Levofloxacin≤2 (S) Ciprofloxacin≤0.3 (S)
Meropenem≤1 (S) Tigecycline≤1 (S)
Piperacillin/Tazobactam≤16 (S) Trimeth/Sulfa≤20 (S)
Trimeth/Sulfa≤2/38 (S)
Tetracycline≤4 (S)
Ticarcillin/clavulanic acid≤16 (S)
Tobramycin≤4 (S)

S: sensitivity, R: Resistance, ESBL: extended spectrum bet-lactamase.

  • 1. Yoon BI, Han DS, Ha US, Lee SJ, Sohn DW, Kim HW, et al. Clinical courses following acute bacterial prostatitis. Prostate Int 2013;1:89-93. ArticlePubMedPMC
  • 2. Jang K, Lee DH, Lee SH, Chung BH. Treatment of prostatic abscess: case collection and comparison of treatment methods. Korean J Urol 2012;53:860-4. ArticlePubMedPMC
  • 3. Lee DS, Choe HS, Kim HY, Kim SW, Bae SR, Yoon BI, et al. Acute bacterial prostatitis and abscess formation. BMC Urol 2016;16:38. ArticlePubMedPMCPDF
  • 4. Kozlowska J, Smith S, Roberts J, Pridgeon S, Hanson J. Prostatic abscess due to Burkholderia pseudomallei: facilitating diagnosis to optimize management. Am J Trop Med Hyg 2018;98:227-30. ArticlePubMed
  • 5. Park KK, Kim SD, Kim YJ, Huh JS. Antibiotic sensitivity of bacterial strains from prostate abscess pus aspirated using ultrasound guidance. Urogenit Tract Infect 2022;17:26-30. Article
  • 6. Choby JE, Howard-Anderson J, Weiss DS. Hypervirulent Klebsiella pneumoniae - clinical and molecular perspectives. J Intern Med 2020;287:283-300. ArticlePubMedPDF
  • 7. Liu JW, Lin TC, Chang YT, Tsai CA, Hu SY. Prostatic abscess of Klebsiella pneumonia complicating septic pulmonary emboli and meningitis: a case report and brief review. Asian Pac J Trop Med 2017;10:102-5. ArticlePubMed
  • 8. Weinberger M, Cytron S, Servadio C, Block C, Rosenfeld JB, Pitlik SD. Prostatic abscess in the antibiotic era. Rev Infect Dis 1988;10:239-49. ArticlePubMed
  • 9. Magill SS, O'Leary E, Janelle SJ, Thompson DL, Dumyati G, Nadle J, et al. Emerging Infections Program Hospital Prevalence Survey Team. Changes in prevalence of health care-associated infections in U.S. hospitals. N Engl J Med 2018;379:1732-44.ArticlePubMedPMC
  • 10. Batra R, Whalen W, Alvarez-Mulett S, Gomez-Escobar LG, Hoffman KL, Simmons W, et al. Multi-omic comparative analysis of COVID-19 and bacterial sepsis-induced ARDS. PLoS Pathog 2022;18:e1010819. ArticlePubMedPMC

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        Urogenit Tract Infect. 2023;18(3):114-118.   Published online December 31, 2023
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      Case of Life-Threatening Pneumonia during the Treatment of a Patient with Acute Bacterial Prostatitis
      Image Image Image Image Image Image
      Fig. 1 (A) On the first day. Chest posteroanterior (PA): no active lung lesion. (B) On the third day. Chest PA: newly appeared diffuse patchy and nodular opacities throughout both lungs.
      Fig. 2 In the contrast-enhanced com-puted tomography scan. (A) The axial view showed prostatic enlargement with heterogeneous enhancement on the admission day. (B) The axial view demonstrated multiple loculated fluid collections and lobulated lesions in the prostate on the seventh day after hospitalization.
      Fig. 3 On the second day, transrectal ultrasound revealed a prostate volume of 152 gm with central gland enlargement and calcifications, and heterogeneous parenchymal echoes were observed in both peripheral zones.
      Fig. 4 Computed tomography scan of the chest showed dense consolidation in both lobes (pneumonia with acute respiratory distress syndrome).
      Fig. 5 On the eighth day of admission to the intensive care unit, transurethral unroofing of the prostate abscess.
      Fig. 6 Transrectal ultrasound showed that the prostate volume decreased to 27.7 gm one month after discharge.
      Case of Life-Threatening Pneumonia during the Treatment of a Patient with Acute Bacterial Prostatitis

      Antibiotic sensitivity of the bacteria identified in the urine and blood cultures

      Urine culture Blood culture
      Bacteria Klebsiella pneumoniae Klebsiella pneumoniae
      Result of sensitivity Ampicillin/Sulbactame≤8/4 (S) ESBL (-)
      Amikacin≤16 (S) Ampicillin≥32 (R)
      Ampicillin>16 (R) Amoxicillin/Clavulanic acid≤2 (S)
      Aztreonam≤4 (S) Piperacillin/Tazobactam≤4 (S)
      Ceftazidime≤1 (S) Ceftizoxime≤4 (S)
      Cefotaxime≤1 (S) Cefoxitin≤4 (S)
      Cefoxitin≤8 (S) Cefotaxime≤1 (S)
      Ceftizoxime≤2 (S) Ceftazidime≤1 (S)
      Ciprofloxacin≤1 (S) Cefepime≤1 (S)
      Cefepime≤2 (S) Aztreonam≤1 (S)
      Cefuroxime≤4 (S) Ertapenem≤0.5 (S)
      Ertapenem≤0.5 (S) Imipenem≤0.3 (S)
      Gentamicin≤4 (S) Amikacin≤2 (S)
      Imipenem≤1 (S) Gentamicin≤1 (S)
      Levofloxacin≤2 (S) Ciprofloxacin≤0.3 (S)
      Meropenem≤1 (S) Tigecycline≤1 (S)
      Piperacillin/Tazobactam≤16 (S) Trimeth/Sulfa≤20 (S)
      Trimeth/Sulfa≤2/38 (S)
      Tetracycline≤4 (S)
      Ticarcillin/clavulanic acid≤16 (S)
      Tobramycin≤4 (S)

      S: sensitivity, R: Resistance, ESBL: extended spectrum bet-lactamase.

      Table 1 Antibiotic sensitivity of the bacteria identified in the urine and blood cultures

      S: sensitivity, R: Resistance, ESBL: extended spectrum bet-lactamase.


      Urogenit Tract Infect : Urogenital Tract Infection
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